A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989367



Internal ID21898710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:34039598..35189734hg38UCSC Ensembl
chr2:34264665..35414800hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg381150137
hg191150136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989367
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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